Translocation into the Nucleus, Mitochondria, and Peroxisomes- Lecture 36 Flashcards

1
Q

What distinguishes transport into the nucleus, mitochondria, and preoxisomes from the secretory pathway?

A

proteins entering these organelles do so after translation in the cytosol

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2
Q

What is the main function of the mitochondria?

A

generation of ATP (which can be used for cellular energy)

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3
Q

MItochondria have their own genome that encodes _____ proteins and RNA components of _______.

A

13

mitochondrial ribosomes

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4
Q

Describe how liver mitochondria differ in appearance from skeletal muscle mitochondria.

A

liver have fewer cristae than skeletal

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5
Q

What are the reactions that are completed in the matrix?

A

oxidation reactions
oxidation of fatty acids
enzymes of urea cycle

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6
Q

What creates a membrane potential across the inner membrane?

A

the movement of protons

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7
Q

Where is the mitochondrial genome contained?

A

in the matrix

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8
Q

What are the differences in coding between the mitochondrial genome and universal genome?

A

AUG is universally a STOP codon, but codes for Tryptophan in mitochondria
AGG is universally an Arginine but becomes a STOP codon in mitochondria

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9
Q

Describe the human mitochondrial genome.

A

circular

16,569 bp

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10
Q

How does mitochondria replicate?

A

divides into two from one existing mitochondria via fission reaction
divide asynchronously

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11
Q

Describe the types of nuclear encoded mitochondrial genes contained in target sequences.

A

15-35 residue N-terminal sequence comprising basic amino acids that are cleaved in the matrix by an endoprotease
non-cleaved internal sequence

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12
Q

Describe how a protein is translocated into the mitochondria.

A

Hsc70 molecular chaperones bind target sequence of protein as it emerges from ribosome –> brings it closer to a specific receptor on the OMM –> proximity to TOM complex allows for the protein to translocate across the outer membrane (still not folded) –> protein is translocated actross the IMM by TIM channels (positive charge in IMS opens the TIM and draws the protein into the channel, where they can be guided further by their Hsc70
once in the matrix, protein folds with help from Hsc60 and Hsc70 and the targeting sequence is cleaved

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13
Q

Provide an example of mitochondrial disease/

A

Leer’s hereditary optic neuropathy(LHON)by missense mutation in subunit 4 of NADH-coQ reductase
results in midlife sudden onset blindness

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14
Q

What is the main role of peroxisomes?

A

fatty acid beta-oxidation resulting in hydrogen peroxide as a biproduct which is metabolized by catalase to water an d oxygen

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15
Q

Describe the structure of peroxisomes.

A

single walled

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16
Q

How do proteins enter the peroxisome?

A
targeting sequence (SKL on the C terminus) is recognized by PGX5 (a soluble receptor) which transports the folded protein into the peroxisome via channel
after entering, the receptor releases and is transported back out
17
Q

The nucleus houses the genetic material to separate it from the cytosol, thereby separating ________ from _______.

A

Transcription

translation

18
Q

What activities occur in the nucleus?

A

transcription, mRNA splicing, DNA replication, and ribosome biosynthesis

19
Q

Describe the structure of the nucleus.

A

surrounded by a double lipid bilayer with the outer one being continuous with the rough ER
perinuclear space between the membranes is contiguous with the lumen of the ER
inner surface is lined with nuclear lamina and punctuated with nuclear pores
a secondary structure inside is called the nucleolus

20
Q

Describe the pathway of genetic material that codes for ribosomes.

A

ribosomal protein genes are transcribed by RNA pol II –> exit the nucleus to be translated by cytoplasmic ribosomes –> proteins reenter the nucleus and bind cytoplasmic ribosomes –> complex reenters the nucleus and is transported to the nucleolus –> assemble rRNA –> pre-ribosomal particles are delivered to the cytosol

21
Q

An ____ is typically ____ amino acids, rich in ____ and ____ and usually contains ____.

A

nuclear localization sequence (NLS)
4-8
Arg, Lys
Pro

22
Q

Describe the nuclear pore complex.

A

eight fold symmetry
contains a central aqueous channel of 9nm diameter and 15 nm length
composed of several ring assemblies that occupy the cytoplasmic face, inner core, and nucleoplasmic face of the structure
filamentous assemblies radiate out from both sides

23
Q

Describe the process of nuclear transport.

A

karyopherins recognize NLS or NES sequences and bind –> complex travels into nucleus via NPC complex –> Ran-GTP binds the karyopherin –> protein dissociates from complex which is exported into the cytosol –> RanGTP is hydrolized to RanGDP by a GAP and re-enters the nucleus via another NPC